Androgen Receptor Inhibitors in the Treatment of Acne Vulgaris: Efficacy and Safety Profiles of Clascoterone 1% Cream.

The purpose of this narrative review is to provide a summary of the clinical trials on the efficacy and safety of clascoterone 1% cream (Winlevi) to grant providers an understanding of which patients will benefit most from this novel topical antiandrogen medication. Clascoterone 1% cream (Winlevi) offers a new and exciting treatment approach for a difficult and common skin condition such as acne vulgaris. This topical androgen antagonist is the first of its kind but will hopefully provoke investigations into other androgen receptor antagonists with similar or better efficacy.

Introduction

Acne vulgaris is an inflammatory skin condition that typically affects teens and adolescents, although it can expand to affect other age groups.1 There are several pathophysiologic pathways in the emergence of acne vulgaris. These pathways involve follicular hyperkeratinization, overactive sebaceous glands, Cutibacterium acnes colonization, and inflammation. Therefore, the role of current acne treatments is to target these specific pathogenic factors.

Anti-androgen medications target overactive sebaceous glands, leading to a reduction in sebum secretion rate.2 Physicians have long been using hormonal agents with anti-androgen effects to treat acne vulgaris. The most commonly prescribed medications are combined oral contraceptives (COCs) and spironolactone. COCs were first introduced in the 1960s for contraceptive use. It was not until 1997 that the first COC, Ortho Tri-cyclen, was approved for acne vulgaris.3 Since then, there have been three more COCs approved by the FDA. These include Estrostep (approved in 2001), Yaz (approved in 2007), and Beyaz (approved in 2010).3 The estrogen in the FDA-approved medications is ethinyl estradiol. Progestins in the formulations for COCs approved for acne differ but include norgestimate, norethindrone acetate, and drospirenone.3 COCs alter acne lesions through disparate pathways. The anti-androgenic effect of COCs is mainly through estrogen’s testosterone synthesis inhibition mechanism.4 However, progestins in birth control also have a function in anti-androgenic effects through antagonistic mechanisms.4 First, COCs, primarily through estrogen, increase the levels of sex-hormone binding globulin, which leads to a decrease in free testosterone available for receptors. Simultaneously, luteinizing hormone inhibition leads to decreased production of testosterone.5 In addition, COCs inhibit the enzyme 5-alpha-reductase, which is responsible for the conversion of testosterone into dihydrotestosterone (DHT). COCs have also been proposed to block testosterone and DHT binding to their corresponding receptors, thus limiting their androgenetic effects on the skin.6

There has been a wide range of clinical trials to assess the efficacy of COCs for acne. Most of these trials showed evidence of reduced acne lesion count in patients on COCs. In trials in which acne lesion count was not reduced, researchers still established an effect on sebum production. COCs were associated with a significant reduction in sebum production in the face.4 Despite significant efficacy in treating acne, COCs carry a more extensive side effect profile than topical therapies. For instance, although infrequent, COCs confer a cardiovascular risk, especially in patients with higher baseline risk. This cardiovascular risk increases with the length of contraceptive use.4 Another uncommon risk to acknowledge when counseling patients for treatment is a cancer risk, specifically breast cancer, which remains controversial.4 More commonly, patients report headaches, menstrual irregularities, and mood lability after initiation of COCs.7

Apart from COCs, spironolactone is a different therapeutic agent used for its anti-androgenic properties. However, it has not received United States Food and Drug Administration (FDA) approval for acne and thus is used off-label. According to the American Academy of Dermatology (AAD), it is considered an alternative treatment in all cases of acne vulgaris from mild to severe.8 Dating back to the 1980s, prospective studies on oral spironolactone have shown statistically significant efficacy against acne vulgaris in women.8–11 Although studies have shown efficacy in spironolactone for acne, they have been small in sample size. A recent retrospective study of 110 patients concluded that spironolactone therapy provided patients with improvement in their acne.11 Similar to COCs, the systemic exposure of oral anti-androgens poses risks for potential side effects. Common side effects are menstrual irregularities, dizziness, breast enlargement, and nausea. Less common side effects associated with spironolactone include hyperkalemia and estrogen-sensitive cancers. However, cancer development has not been well-established in humans and instead has been shown in animal studies.8 Many of the risks conferred by hormonal agents arise from their systemic exposure. In addition, male patients do not tolerate associated gynecomastia when taking spironolactone for acne.12

On the contrary, systemic exposure can be limited through the use of topical applications. They reduce the risk for potential side effects, although they have sometimes been considered as less efficacious in more severe cases of acne vulgaris.13

Topical spironolactone has been postulated for use in acne vulgaris. In one small single-blinded study, topical spironolactone 2% solution was shown to significantly reduce comedone count compared to no effect on comedones by clindamycin.14 Additionally, compared to clindamycin, the topical application of spironolactone resulted in a more significant reduction of patients’ Acne Severity Index (ASI). Similar results have been achieved in other clinical trials.15,16

Another way to target the increased levels of DHT in acne pathogenesis is through inhibition of 5-alpha-reductase, the enzyme responsible for peripherally converting testosterone to DHT.16 Finasteride is a 5-alpha-reductase inhibitor that is mainly used in benign prostatic hyperplasia (BPH) and male pattern hair loss. However, there have been studies examining its use for acne vulgaris. For example, in one clinical trial done on hyperandrogenic women with moderate-severe acne, finasteride was beneficial for decreasing Cook Score (an acne severity index that uses photographs to document acne severity and is scored from 0–8), although less beneficial than other anti-androgens such as flutamide.17 In a more recent prospective study, the efficacy of finasteride was compared to montelukast for moderate acne in women. The study results showed that finasteride is more efficacious in treating moderate acne than montelukast. Specifically, at the end of the study period (12 weeks), 88% of patients on finasteride had near-total clarity of their acne compared to 76% of patients in the montelukast group. For patient satisfaction, the finasteride group reported 80% satisfaction at the end of the 12 weeks, whereas the montelukast group had a 66.7% satisfaction rate.16

A novel topical antiandrogens for use in acne vulgaris is Cortexolone 17α-propionate (Clascoterone or CB-03-01). Clascoterone 1% cream (Winlevi) is a steroidal topical androgen receptor inhibitor hypothesized to work through competitive inhibition of DHT receptors within the sebaceous glands and hair follicles.7,15 The structure of clascoterone resembles other hormonal agents used for acne vulgaris (Figure 1). The primary metabolite of clascoterone is cortexolone or 11-deoxycortisol, an inactive form.18 In regards to excretion, clascoterone is hypothesized to be hydrolyzed in the skin’s epidermis upon topical application. During in vitro studies, clascoterone 1% cream (Winlevi) was significantly more efficacious in inhibiting inflammatory cytokine production from sebocytes than spironolactone.1 Clascoterone 1% cream (Winlevi) was approved for male and female patients, 12 years and older, by the United States FDA on August 27, 2020.7,15 This novel treatment provides physicians with more options when treating such common skin conditions such as acne. It gives practitioners an anti-androgen treatment, which can be used in males without systemic side effects. Notably, there are no human studies on clascoterone 1% cream (Winlevi) use during pregnancy and breastfeeding. However, animal studies conducted on rats showed organ malformations when subcutaneous doses at 8 to 39 times the recommended dose for humans were used.19

Figure 1

Chemical structures of clascoterone (left) and spironolactone (right) created with MolView an open-source web-application. Both structures are steroid structures that are comprised of a four-ring backbone: three cyclohexane rings and one cyclopentane ring. The molecular formula for clascoterone is  C24H34O5, whereas the molecular formula for spironolactone is C24H32O4S.

With more options in acne treatment, it is imperative that prescribing physicians understand the populations and outcomes in which this drug was studied. Therefore, the objective of this narrative review is to provide a summary of the clinical trials on the efficacy and safety of clascoterone 1% cream (Winlevi) to grant providers an understanding of which patients will benefit most from this novel topical anti-androgen medication.

Experimental Studies

In the United States (US), the first clinical trial on clascoterone 1% cream (Winlevi) started in June 2012.20 Since then, there have been a total of 6 clinical trials completed on the use of clascoterone (Winlevi) for acne vulgaris.20 As described above, orally administered androgen receptor inhibitors have shown efficacy in treating the effects that testosterone and DHT have on the skin and skin appendages but they have potential systemic consequences. On the contrary, topical androgen antagonists have the potential to exhibit activity locally with reduced risks of systemic exposure. Before human studies, Celasco et al examined the systemic effects of cortexolone 17a-propionate in rats and found that while there were strong local antagonistic effects, there was no evidence of systemic antagonistic effects. For 21 days, the researchers applied the experimental drug to the right flank with a microsyringe at concentrations of 100–200- 400 ug/animal dissolved in 0.05 mL of acetone containing 4 ug of testosterone propionate (TP).21 There was a dose-dependent flank organ inhibition, with increased doses resulting in greater inhibition and the highest inhibition of 84% was achieved with the 400 ug dose. Moreover, the researchers did not find evidence of irritation or damaging effects to the skin, thus concluding that it is well-tolerated when topically applied. To assess the systemic effects, the researchers used a separate group of rats, which were injected subcutaneously for seven days at a daily dose of 0.2–1.5 mg/animal in 0.2 mL of a suspending vehicle. After the seven days with injections, the animals were euthanized and the ventral prostate, seminal vesicles, and levator ani muscles were isolated in order to assess the effects of the experimental drug on them. The animals were simultaneously injected with TP on the contralateral side. In conclusion, cortexolone 17a-propionate was unable to completely antagonize the effects of the TP.21 The drug was also devoid of toxic effects on the rats evident by the lack of spontaneous deaths or clinical symptoms during their study. The researchers hypothesize that the absence of systemic effects is, in part, due to a fast hydrolysis by tissues into the inactive parent compound cortexolone.21

Clinical Trials

The findings from a pilot study in 2011 reinforced the use of clascoterone 1% cream for acne. A total of 77 men with facial acne were enrolled in this randomized, double-blind study. In summary, clascoterone 1% cream (Winlevi) was significantly better than placebo in reducing inflammatory lesion count (ILC), acne severity index (ASI), and total lesion count (TLC). Compared to tretinoin 0.05% cream, clascoterone 1% cream (Winlevi) was clinically more effective, but not statistically significant, in reducing TLC and ASI.22 Contrastingly, CB-03-01 was significantly better in reducing inflammatory lesion count compared to tretinoin cream at week 6 (p= 0.0374) The application involved applying the cream nightly for 8 weeks. Additionally, clascoterone 1% cream (Winlevi) also demonstrated a quicker time to the beneficial effects than placebo and tretinoin. Treatment with clascoterone 1% cream (Winlevi) resulted in a 50% improvement of TLC in a median of 43.5 days, whereas the median time for 50% improvement of TLC for tretinoin and placebo were 57 and 58 days, respectively (p= 0.0199). For ILC, the time to 50% improvement was a median of 36.5, 44, and 58 days for clascoterone 1% cream (Winlevi), tretinoin, and placebo, respectively (p= 0.0490). Compared to tretinoin, clascoterone 1% cream (Winlevi) exhibited better tolerability as evidenced by the irritancy score. Patients treated with tretinoin and placebo experienced worsening in their irritancy score in the first 2 weeks of treatment compared to clascoterone 1% cream (Winlevi) (p= 0.0412). Although this study included a small sample of patients, it reinforced findings from previous studies on animals and fortified the need for larger-scale clinical trials.22

To further assess safety in human subjects, a phase two trial was conducted in which researchers investigated the pharmacokinetic properties and hypothalamic-pituitary-adrenal (HPA) axis response to clascoterone 1% cream. The study participants consisted of a cohort of 42 subjects who were 12 years of age and older and were diagnosed with moderate-severe acne according to the Investigator’s Global Assessments [IGA] (grade 3–4). The participants were divided into two cohorts. Cohort 1 was those subjects who were older than 18 years of age whereas Cohort 2 consisted of participants aged 12–18. The medication was applied twice daily for 14 days after which a Cosyntropin Stimulation Test was completed to assess HPA axis suppression and compared to the response on day 1 of the trial. Post-stimulation cortisol levels less than 18 ug/dL were considered to be suppressed levels. Simultaneously, the pharmacokinetics of the medication was assessed through concentration-time profiles of clascoterone and cortexolone (the clascoterone metabolite) in plasma. On day 14, 42.7% of the 42 subjects showed an abnormal HPA axis suppression evidenced by post-stimulation cortisol levels between 14.9 ug/dL and 17.7 ug/dL. However, the cortisol levels returned to normal four weeks after the Cosyntrophin Stimulation Test. Additionally, although cortisol levels were in an abnormal range, there were no clinical signs or symptoms of adrenal suppression in these participants.23 In regards to the pharmacokinetic properties of clascoterone 1% cream (Winlevi), steady-state concentrations in plasma were reached by the fifth day with the mean maximum concentration of 4.4 ug/dL and 4.7 ug/dL in the two cohorts, respectively. The levels of cortexolone stayed below levels of quantitation throughout the study period. Secondary endpoints of the study included local and systemic reactions, clinical laboratory testing, physical exam, and vital signs. There were local skin reactions noted of mild intensity with one case of moderate pruritus. In total, there were nine adverse reactions with two of them being classified as definitely related to the topical medication and four as probably related.23

In a similar study, varying doses of the topical medication were studied for its efficacy and safety. Researchers studied clascoterone cream 0.1%, 0.5%, and 1% twice daily, as well as 1% daily and vehicle (daily and twice daily). Of note, the vehicle cream was formulated to contain and feel the same as the experimental drug but without the active ingredient cortelexone-17a-propionate. Both topical medications (experimental and vehicle) contained cetyl alcohol, citric acid monohydrate, edetate disodium, monoglycerides, mineral oil, polysorbate 80, propylene glycol, purified water, and vitamin E. Efficacy was determined using IGA, total acne lesion counts, and subject satisfaction with treatment. Safety was assessed through local and systemic adverse events, physical exam, vital signs, lab tests, local skin reactions, and electrocardiograms. Subjects were considered to have a successful treatment if their IGA score achieved a 0 or 1, which corresponds to clear or mostly clear, and/or if there was a two-grade improvement in the IGA score from baseline. At the end of 12 weeks, treatment success was highest for the groups who received 1% and 0.1% twice daily. The group receiving the 1% dose achieved the greatest median change from baseline in inflammatory and non-inflammatory lesions with a change in −13.5 and −17.5, respectively. In regards to safety, adverse events were mostly classified as mild and did not differ among different treatment groups or vehicle. For example, there was more than one adverse event in 18.6% of participants in the 1% twice-daily treatment group, while 22.7% participants in the vehicle group and 25% in the 0.1% twice-daily groups experienced at least 1 adverse event. The most common adverse event was a local skin reaction consisting of mild erythema, specifically 32.6% of subjects experienced this local skin reaction throughout the study period. Although these findings show that all tested doses of the clascoterone cream were well-tolerated, they conclude that the most favorable dose of clascoterone cream would be 1%.24

The findings from phase three trials of clascoterone 1% cream (Winlevi) continued to parallel previous findings. In two phase-three trials of patients 9 years and older, patients treated with clascoterone 1% cream (Winlevi) displayed greater treatment success than patients treated with vehicle.25 Treatment success was defined as a 2-point reduction in IGA score in addition to a score of 0 or 1. Other primary endpoints were absolute change from baseline in total lesion counts (TLC), noninflammatory lesion counts (NILC), and inflammatory lesion counts (ILC). In the experimental cohort of one trial, 18.4% of patients achieved treatment success at week 12 compared to 9.0% in the vehicle cohort (p <0.001). In the second trial, 20.3% of patients in the experimental group achieved treatment success at week 12 versus 6.5 of patients receiving the vehicle (p <0.001). Additionally, there was a greater absolute change in the NILC and ILC at week 12 in the experimental cohort in both trials compared to vehicle. Patients in the first trial on experimental treatment achieved an absolute change of −19.4 and −19.3 in NILC and ILC, respectively. Whereas patients on vehicle achieved an absolute change of −13.0 and −15.5 in NILC and ILC, respectively. Patients on the experimental treatment saw a greater percent change in non-inflammatory lesion counts, inflammatory lesion counts, and total lesion counts, which were considered secondary endpoints.25 Similar to the study by Mazzeti et al, the most frequent local skin reaction was erythema. Mild nasopharyngitis, oropharyngeal pain, and headaches were the most common treatment adverse effects in both trials. In addition, both trials cited application site dryness as an adverse effect related to clascoterone 1% cream (Winlevi). Five patients receiving clascoterone 1% cream (Winlevi) and 12 patients receiving vehicle cream discontinued the treatment due to the treatment-emergent adverse effects. The adverse effects that resulted in discontinuation were mild application site hypersensitivity, oropharyngeal pain, sebaceous hyperplasia, facial acute contact dermatitis, and depigmentation of the hair on the nose. Finally, there were no cases of systemic adverse effects in either trial confirming that clascoterone 1% cream (Winlevi) has only local antiandrogenic activity.10 Although clinically significant, these studies did not use adjuvant acne therapies. Future studies should aim to include complementary acne therapies such as topical antibiotics or topical retinoids to determine the most optimal therapeutic approach.

The most recent clinical trial conducted on this novel medication was completed to assess for long-term effects of clascoterone 1% cream (Winlevi) applied twice daily. Thus far, the clinical trials focused on treatments for no longer than 12 weeks. In this trial, the medication was applied twice daily for up to 9 months. Subjects were evaluated for adverse events and local skin reactions at intervals of 1, 3, 6, and 9 months. About 18% of 347 subjects developed 191 treatment-emergent adverse events. Nasopharyngitis, which was the most frequently reported treatment-emergent adverse event, was reported in 20 out of 179 patients. This was similar to the adverse effect cited in the two trials by Herbert et al. The adverse events were similar among both treatment and vehicle groups, coinciding with the previous phase three clinical trials. However, a higher number of adverse events occurred in subjects who were originally assigned to the experimental group. Study discontinuation due to an adverse event was observed in 9 participants. Some of the adverse events experienced by these participants were moderate application site swelling, moderate dryness, and a severe suicide attempt. Although there were adverse events and local skin reactions such as erythema, the authors conclude that the safety profile of the medication could still be considered favorable. These are relatively low frequency of treatment-emergent adverse events and most were mild or moderate.26 Table 1 includes a summary of the data presented.

Table 1

Summary of Experimental Studies and Clinical Trials

Author	Study Design	Study Population	Interventions	Controls	Results	Conclusions	Limitations
Celasco et al (2004)21	Experimental animal studies	Syrian Golden hamsters and Wistar rats	CB-03-01, 100–200-400 ug/animal dissolved in 0.05 mL of acetone with 4 ug of TP or 4 ug of DHT	Parent cortexelone and progesterone at a daily dose of 400 ug/animal dissolved in 0.05 mL of acetone containing 4ug of TP, 0.05 mL of acetone, vehicle, TP (4ug), or DHT (4 ug)	Topical CB-03-01 in TP had 84% inhibition of the flank organ enlargement (p <0.01).CB-03-01 resulted in about 3x more potent than flutamide and 2x more potent than finasteride. CB-03-01 was completely unable to antagonize the effects of TP on the organs.	CB-03-01 has strong topical activity for androgen-dependent skin disorders with absence of systemic effects.	Lack of data in human subjects.
Trifu et al (2011)22	Pilot, randomized, double-blind comparative trial.	Men with IGA scores of 2–3	CB-03-01	Tretinoin 0.05% cream, placebo cream	CB-03-01 was associated with significantly better TLC (P = 0.0017), ILC (P = 0.0134) and ASI(P = 0. 0090) scores when compared to to placebo. It was also associated with significantly better TLC, ILC, and ASI scores compared to tretinoin.	CB-03-01 is useful for treating acne vulgaris in men with score 2–3 on IGA.	Men onlySmall sample size
Mazzetti et al (2019)23	Open label phase 2a RCT	Male and females >11 years old with IGA 3–4 acne vulgaris	Clascoterone 1% cream	None	Three subjects (3/42,7%), 1 adult and 2 adolescents, demonstrated an abnormal HPA axis response with post-stimulation serum cortisol levels ranging from 14.9 to 17.7 μg/dL at day 14. All returned to normal HPA axis function, four weeks after day 14. None showed clinical evidence of adrenal suppression.	Clascoterone 1% cream does not cause HPA axis dysfunction.	Lack of data on subgroups such as different racial and age groupsITT done on only 54% females and 46% males
Mazzetti et al (2019)24	Phase 2b RCT	Male and females > 11 years old with acne vulgaris	Clascoterone 0.1% BID, 0.5% BID, or 1% QD or BID	Vehicle QD or BID	Treatment success at week 12 were highest for the 1% BID (6/70,8.6%) and 0.1% BID (6/72, 8.3%) groups versus vehicle (2/75, 2.7%). Absolute change in inflammatory (P=0.0431)and non-inflammatory (P=0.0303) lesions was statistically significant among the treatment groups. The median change from baseline at week 12 in inflammatory and non-inflammatory lesions was greatest in the 1% BID group-13.5 and −17.5, respectively.	The most effective dose of topical clascoterone is 1% cream.	Lack of data on subgroups such as different racial and age groups
Herbert et al (2020)25	Phase 3 RCT	Male and female patients 9 years and older with IGA 3–4 acne vulgaris	Clascoterone cream 1%	Vehicle	Clascoterone 1% cream in two of the sites had treatment success rates at week 12 of 18.4% and 20.3% vs 9.0% and 6.5% with vehicle (P <0.001). Treatment with the intervention resulted in significant reduction in the absolute noninflammatory lesion counts from baseline to week 12 (−19.4) (P< 0.001) vs −13 with vehicle (P<0.001). There were also reductions in ILC from baseline to −19.3 compared to −15.5 wit vehicle (P<0.001). Adverse events were mild and at low rates.	Clascoterone 1% cream is associated with favorable efficacy and safety with minimal risks for adverse events	Lack of subgroup analysis on race/ageLack of concomitant acne therapies
Eichenfield et al (2020)26	Open-label, long-term extension study	Patients from one of the phase 3 trials conducted on clascoteron1% cream	Clascoterone1% cream BID	N/A	18.1% patients experienced TEAEs. Most frequent TEAE was nasopharyngitis (n = 20). A totalof 19 test article-related TEAEs occurred in 14 patients; of these, 9 experienced 9 TEAEs leading todiscontinuation. There were 7 serious TEAEs in 6 individuals, none were treatment related. 1 seriousTEAE led to study discontinuation. Overall, treatment-emergent local skin reactions occurred in 18.1%. The most frequent local skin reactions were erythema, scaling/dryness,and pruritus, and most were trace/minimal or mild in severity.	There was a low frequency of TEAEs over 9 months of clascoterone 1% cream use.	No data on safety with concomitant acne therapies.

Abbreviations: ASI, acne severity index; BID, twice daily; CB-03-01, cortexolone-17a-propionate; DHT, dihydrotestosterone; HP, hypothalamic-pituitary-adrenal; IGA, Investigator’s Global Assessment; ILC, inflammatory lesion count; ITT, intention-to-treat; QD, once daily; RCT, randomized-controlled trial; TEAEs, treatment-emergent adverse events; TP, testosterone propionate; TLC, total lesion count.

Discussion

In female and male ≥ 9 year old patients with moderate-severe acne vulgaris, there is strong evidence favoring the clinical efficacy and safety of clascoterone 1% cream (Winlevi) twice daily. In summary, one pilot study, two Phase 2 trials, and three Phase 3 trials shared complementary findings for this new medication. Recently FDA approved, this new medication will slowly start being incorporated by prescribing physicians in the US. It’s currently not approved for use outside the US, and the European Medicines Agency has not listed it as a medication under investigation for human use.

Interestingly, clascoterone 1% cream (Winlevi) has been proposed to be effective in treating other skin conditions such as hidradenitis suppurativa (HS), androgenetic alopecia, and hirsutism. In an experimental study on dermal papilla cells in vitro, clascoterone was shown to decrease transcription of androgen-receptor-dependent genes. It was also shown to be more powerful at inhibiting interleukin-6 (IL-6) synthesis from DHT-stimulated cultures when compared to another androgen receptor antagonist, enzalutamide.24 IL-6 is a cytokine produced in the body in response to infections, tissue injury, and inflammation. It has been associated with the chronic inflammation and autoimmunity pathogenesis behind rheumatoid arthritis and juvenile idiopathic arthritis.27 Der Sakkistian et al explain the rationale for using clascoterone 1% cream in HS is due to its ability to inhibit DHT, which is the androgen most likely responsible for the clinical signs of HS. In one case series, 85% of women on spironolactone demonstrated a clinical response of their HS. Similar or better findings could be achieved with clascoterone due to the fact that this novel medication targets more of the initial pathogenesis of HS such as follicular plugging.28 A similar rationale has been proposed for its use in androgenic alopecia. That is the inhibition of DHT, which is known to play an active role in the development of androgenic alopecia. Moreover, during in vitro studies, clascoterone was found to have similar efficacy to finasteride, which is often used in the treatment of androgenic alopecia. The benefit of clascoterone 1% cream over finasteride and similar medications relates to its local reaction and favorable side effect profile, especially for males.29 Treatment of acne vulgaris commonly requires regimens involving two or more medications. For instance, when treating mild-moderate acne, topical antibiotics are often used concomitantly with benzoyl peroxide or topical retinoids to prevent antibiotic resistance.12 Due to its recent approval for acne, there is a paucity of data on the efficacy and safety of clascoterone 1% cream (Winlevi)when combined with other acne medications. Future studies should focus on addressing the clinical effects that concomitant use of other acne medications has on the efficacy of clascoterone 1% cream (Winlevi). In the AAD 2016 guideline for acne, it was established that there is a considerable amount of gap in knowledge in regards to acne treatment in skin of color.8 The phase 3 clinical trials on clascoterone 1% cream (Winlevi) were composed of mostly White patients (84.4% in one trial and 96.6% in the second trial) with post-inflammatory hyperpigmentation (PIH) rarely being reported. However, for patients with skin of color, PIH is a more common concern when treating acne. In fact, the development of PIH has been associated with irritation from acne treatment. Future studies should investigate how effective this medication may be for people belonging to racial/ethnic groups such as African-Americans, Hispanics, Native Americans, etc. In one survey study, 42% of nonwhite patients cited resolution of PIH as one of the most important goals when undergoing acne therapy.30 Additionally, although two clinical trials focused on patients 9 years old and older and showed beneficial effects, the FDA has approved this medication for patients ≥ 12 years-old. It is possible that this is due to the small number of patients in the cohort of 9–11 year olds. Specifically, there were only 19 patients in the 9–11 year old cohorts.25

There are several limitations to the studies included in this review. First, the sample sizes did not allow for further subanalysis on different populations. It is possible that the results for different groups may differ.22–26 Secondly, none of the clinical trials assessed concomitant acne therapies with clascoterone. There is a possibility that the most optimal results on acne severity are achieved through a compounded action with different medications.22–26

Conclusion

In conclusion, clascoterone 1% cream (Winlevi) offers a new and exciting treatment approach for a difficult and common skin condition such as acne vulgaris. Not only do clinical trials show efficacy for reduction in total acne lesion counts, it has a significantly tolerable safety profile even at nine months of treatment. At this time, this topical androgen antagonist is the first of its kind but will hopefully provoke investigations into other androgen receptor antagonists with similar or better efficacy.